HMGCL Gene 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency NGS Genetic DNA Test
The HMGCL Gene 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency NGS Genetic DNA Test is a vital diagnostic tool used to identify potential genetic disorders related to the HMGCL gene. This test plays a significant role in diagnosing metabolic disorders, allowing for timely interventions and management strategies that can greatly enhance the quality of life for affected individuals.
What the Test Measures/Detects
This genetic test detects mutations in the HMGCL gene that may lead to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency, a rare metabolic disorder. By identifying these mutations, healthcare providers can better understand the patient’s condition and tailor treatment plans accordingly.
Who Should Consider This Test?
This test is particularly recommended for individuals who:
- Have a family history of metabolic disorders.
- Exhibit symptoms such as hypoglycemia, metabolic acidosis, or developmental delays.
- Are undergoing genetic counseling for a suspected metabolic condition.
Benefits of Taking the Test
- Early diagnosis can lead to better management of metabolic disorders.
- Informs treatment options and dietary modifications to prevent complications.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the HMGCL Gene 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency NGS Genetic DNA Test will be discussed with your healthcare provider, who will explain the implications of the findings and guide you on the next steps. It is essential to consider the results in the context of clinical history and symptoms.
Test Name and Price
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| HMGCL Gene 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To schedule your HMGCL Gene 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +2348110567037. Our team is ready to assist you with the booking process and provide any additional information you may need.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical history of the patient who is going for the test and a genetic counselling session to draw a pedigree chart of family members affected with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
Don’t wait for symptoms to appear; take proactive steps towards your health today!
